2024-04-28 01:56:49, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NR_034126 1542 bp RNA linear PRI 19-APR-2022 DEFINITION Homo sapiens long intergenic non-protein coding RNA 1160 (LINC01160), long non-coding RNA. ACCESSION NR_034126 VERSION NR_034126.1 KEYWORDS RefSeq. SOURCE Homo sapiens (human) ORGANISM Homo sapiens Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo. REFERENCE 1 (bases 1 to 1542) AUTHORS Ai J, Tan G, Wang T, Li W, Gao R, Song Y, Xiong S and Qing X. TITLE Transcription factor STAT1 promotes the proliferation, migration and invasion of nasopharyngeal carcinoma cells by upregulating LINC01160 JOURNAL Future Oncol 17 (1), 57-69 (2021) PUBMED 33263259 REMARK GeneRIF: Transcription factor STAT1 promotes the proliferation, migration and invasion of nasopharyngeal carcinoma cells by upregulating LINC01160. COMMENT PREDICTED REFSEQ: This record has not been reviewed and the function is unknown. The reference sequence was derived from AL391063.14. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-183 AL391063.14 56071-56253 c 184-257 AL391063.14 52564-52637 c 258-389 AL391063.14 52304-52435 c 390-453 AL391063.14 50127-50190 c 454-1542 AL391063.14 46942-48030 c FEATURES Location/Qualifiers source 1..1542 /organism="Homo sapiens" /mol_type="transcribed RNA" /db_xref="taxon:9606" /chromosome="1" /map="1p13.2" gene 1..1542 /gene="LINC01160" /note="long intergenic non-protein coding RNA 1160" /db_xref="GeneID:100129269" /db_xref="HGNC:HGNC:49525" ncRNA 1..1542 /ncRNA_class="lncRNA" /gene="LINC01160" /product="long intergenic non-protein coding RNA 1160" /db_xref="GeneID:100129269" /db_xref="HGNC:HGNC:49525" exon 1..183 /gene="LINC01160" /inference="alignment:Splign:2.1.0" variation 1 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658850154" variation 6..13 /gene="LINC01160" /replace="gcc" /replace="gcccggcc" /db_xref="dbSNP:1658849876" variation 6 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1462794695" variation 9 /gene="LINC01160" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1467428528" variation 10 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:1571495350" variation 13 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1407347845" variation 14 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1303992081" variation 16 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:2101077846" variation 17 /gene="LINC01160" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1344925269" variation 19 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:1658849610" variation 21 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1273052544" variation 23 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:6660669" variation 27 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658849435" variation 31 /gene="LINC01160" /replace="" /replace="t" /db_xref="dbSNP:1658849377" variation 32..35 /gene="LINC01160" /replace="ggg" /replace="gggg" /db_xref="dbSNP:200215971" variation 33 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1279995879" variation 34 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1326998736" variation 35 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1571495334" variation 36 /gene="LINC01160" /replace="" /replace="a" /db_xref="dbSNP:1249462723" variation 37 /gene="LINC01160" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1571495332" variation 38 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:1330570941" variation 40 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:903221067" variation 43 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1046134569" variation 44 /gene="LINC01160" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1222841941" variation 45 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1658848819" variation 46 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658848770" variation 49 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1218223382" variation 50 /gene="LINC01160" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1265932380" variation 52 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1367945602" variation 53 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:950329821" variation 54..57 /gene="LINC01160" /replace="ccc" /replace="cccc" /db_xref="dbSNP:1557864127" variation 57 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1658848450" variation 58 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1371637272" variation 59 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1438363264" variation 65 /gene="LINC01160" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1473979197" variation 67 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1164401621" variation 68 /gene="LINC01160" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1286086646" variation 71 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1393482324" variation 73 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:1321093945" variation 74 /gene="LINC01160" /replace="g" /replace="gattg" /db_xref="dbSNP:1458790192" variation 74 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:1300192096" variation 75..76 /gene="LINC01160" /replace="" /replace="cgagattgca" /replace="ctcccaaagtgccgagattgca" /db_xref="dbSNP:1658847838" variation 76 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1381521280" variation 77 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658847731" variation 79 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1571495287" variation 81 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1293357454" variation 82 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:368833389" variation 85 /gene="LINC01160" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:894709520" variation 86 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1241673994" variation 87 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:1260860940" variation 88 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658847284" variation 89..90 /gene="LINC01160" /replace="" /replace="tg" /db_xref="dbSNP:1571495272" variation 89 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1349726777" variation 90 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1400197470" variation 91 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:376994913" variation 92 /gene="LINC01160" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1426064412" variation 93 /gene="LINC01160" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1195758176" variation 94 /gene="LINC01160" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1452919406" variation 97 /gene="LINC01160" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1252809913" variation 98 /gene="LINC01160" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1443075277" variation 102 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1160698842" variation 106 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1189754629" variation 110 /gene="LINC01160" /replace="a" /replace="t" /db_xref="dbSNP:1364389160" variation 112 /gene="LINC01160" /replace="g" /replace="gggcggccg" /db_xref="dbSNP:1453187062" variation 114 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1571495240" variation 115 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1286996818" variation 116 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1055903654" variation 117 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1453058072" variation 118 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1335917232" variation 125 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1487172490" variation 126 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1448456532" variation 127..180 /gene="LINC01160" /replace="gccgccccgtctga" /replace="gccgccccgtctgagaagtgaggagaccctccgcctcgcagccgcccc gtctga" /db_xref="dbSNP:1658843676" variation 127 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:1658845850" variation 129 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1307262099" variation 130 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:2101077695" variation 131..134 /gene="LINC01160" /replace="ccc" /replace="cccc" /db_xref="dbSNP:1236319380" variation 132 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:372792238" variation 134 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658845583" variation 135 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:930780512" variation 137 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658845465" variation 138 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:1658845412" variation 139 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658845359" variation 140 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:1658845299" variation 141 /gene="LINC01160" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1326366496" variation 143 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:1658845200" variation 144 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1204698520" variation 148 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1658845080" variation 151 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:555174849" variation 152 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:1460263576" variation 157 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:1658844905" variation 158 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1214369176" variation 159 /gene="LINC01160" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1418556504" variation 160 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1157059692" variation 164 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:75920601" variation 166 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:1175630801" variation 167 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:1658844488" variation 169 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1281957064" variation 170 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:971879621" variation 171..174 /gene="LINC01160" /replace="ccc" /replace="cccc" /db_xref="dbSNP:1658844199" variation 171 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658844305" variation 173 /gene="LINC01160" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:940429188" variation 174 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1369932203" variation 175 /gene="LINC01160" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1298126045" variation 176 /gene="LINC01160" /replace="a" /replace="t" /db_xref="dbSNP:1437171642" variation 180 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1224592498" variation 181 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1263095530" exon 184..257 /gene="LINC01160" /inference="alignment:Splign:2.1.0" variation 185 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:999473772" variation 189 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1215043825" variation 195 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658737421" variation 198 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:903755682" variation 199 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658737285" variation 203 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:968518761" variation 206 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658737125" variation 207 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:1658737051" variation 210 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658736989" variation 211 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1557862869" variation 216 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1396162324" variation 218 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1193465027" variation 220 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:768835455" variation 223 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658736623" variation 227 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658736556" variation 230 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:575577657" variation 232 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:151282900" variation 236 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1407325391" variation 242 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658736273" variation 246 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:1658736204" variation 248 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658736129" variation 250 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658736058" exon 258..389 /gene="LINC01160" /inference="alignment:Splign:2.1.0" variation 258 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658733307" variation 259 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1283450960" variation 261 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1003745941" variation 262 /gene="LINC01160" /replace="" /replace="t" /db_xref="dbSNP:1658733074" variation 262 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:1658733010" variation 265 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658732934" variation 268 /gene="LINC01160" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:939450397" variation 270..273 /gene="LINC01160" /replace="actg" /replace="actgactg" /db_xref="dbSNP:1348360461" variation 273 /gene="LINC01160" /replace="" /replace="g" /db_xref="dbSNP:1658732663" variation 273 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1276888412" variation 274 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658732545" variation 279 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:905399339" variation 284 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:2786993" variation 285..286 /gene="LINC01160" /replace="c" /replace="cc" /db_xref="dbSNP:1217457173" variation 294 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658731708" variation 298 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:187724626" variation 299 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658731589" variation 310 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:1195505231" variation 320 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658731390" variation 328 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:941639409" variation 331 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:371572477" variation 333 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:909596180" variation 335 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658731013" variation 336 /gene="LINC01160" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1658730945" variation 338 /gene="LINC01160" /replace="a" /replace="t" /db_xref="dbSNP:1658730870" variation 345 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:2101074488" variation 346 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658730819" variation 354 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658730782" variation 357 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1170794667" variation 361 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:1658730702" variation 363 /gene="LINC01160" /replace="a" /replace="t" /db_xref="dbSNP:1658730661" variation 364 /gene="LINC01160" /replace="a" /replace="t" /db_xref="dbSNP:1658730614" variation 367 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1571492922" variation 371 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:2101074477" variation 372 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1571492918" variation 374 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658730492" variation 379 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:1571492916" variation 382 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1046735278" variation 383 /gene="LINC01160" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:910112662" variation 387 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658730071" variation 388 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:985659060" exon 390..453 /gene="LINC01160" /inference="alignment:Splign:2.1.0" variation 391 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658686593" variation 393 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:901432581" variation 394 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:746963525" variation 400..406 /gene="LINC01160" /replace="aa" /replace="aaatgaa" /db_xref="dbSNP:2101072999" variation 403..424 /gene="LINC01160" /replace="tgaa" /replace="tgaagactgacttgatcctgaa" /db_xref="dbSNP:1658686238" variation 407 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:879613679" variation 412 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658686362" variation 419 /gene="LINC01160" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1310703281" variation 432 /gene="LINC01160" /replace="a" /replace="t" /db_xref="dbSNP:1376828328" variation 433 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1222357669" variation 437 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1281208399" variation 443 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658686034" variation 448 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1013245089" variation 451 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658685936" variation 453 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658685889" exon 454..1542 /gene="LINC01160" /inference="alignment:Splign:2.1.0" variation 455 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1487638834" variation 460 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658641526" variation 461 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1206929385" variation 463 /gene="LINC01160" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:946116944" variation 468 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658641309" variation 470 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1571490786" variation 471 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:546548214" variation 475 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:775416226" variation 476 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:75455974" variation 477 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1162719904" variation 481 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1347718215" variation 486 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:1455061765" variation 487 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658640832" variation 490 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1288918539" variation 491 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:980075918" variation 496 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1318110057" variation 500 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1279730793" variation 501 /gene="LINC01160" /replace="" /replace="a" /db_xref="dbSNP:959223962" variation 504 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658640544" variation 512 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:554307397" variation 513 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1295959360" variation 516 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658640414" variation 519 /gene="LINC01160" /replace="a" /replace="t" /db_xref="dbSNP:2101071509" variation 521 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:776117330" variation 522 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658640315" variation 525 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658640269" variation 527 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658640224" variation 529 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658640164" variation 539 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1385633500" variation 541 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658640073" variation 542 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1224927325" variation 543 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:368344540" variation 544 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658639840" variation 550 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:969933246" variation 552 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1024115471" variation 554 /gene="LINC01160" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1314828132" variation 559 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1320106896" variation 563 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658639564" variation 568 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658639510" variation 571 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1658639463" variation 572 /gene="LINC01160" /replace="a" /replace="t" /db_xref="dbSNP:1658639417" variation 575 /gene="LINC01160" /replace="a" /replace="t" /db_xref="dbSNP:1334727924" variation 578 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1658639320" variation 579 /gene="LINC01160" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1241521570" variation 587 /gene="LINC01160" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:144119020" variation 588 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1403824882" variation 591 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1658639059" variation 596 /gene="LINC01160" /replace="a" /replace="t" /db_xref="dbSNP:1485548713" variation 597..605 /gene="LINC01160" /replace="aaaaaaaa" /replace="aaaaaaaaa" /replace="aaaaaaaaaa" /db_xref="dbSNP:973651819" variation 598 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1206922558" variation 599 /gene="LINC01160" /replace="a" /replace="t" /db_xref="dbSNP:1658638927" variation 600 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658638870" variation 603 /gene="LINC01160" /replace="a" /replace="t" /db_xref="dbSNP:1658638829" variation 605 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:1244843455" variation 606 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1411419609" variation 609 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1420488668" variation 612 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1557861760" variation 616 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:950815194" variation 617 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1026363248" variation 618 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:1658638414" variation 619 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658638372" variation 624..631 /gene="LINC01160" /replace="aact" /replace="aactaact" /db_xref="dbSNP:1169913251" variation 629 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:1424560846" variation 635 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:568494379" variation 636 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658638154" variation 639 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1372930987" variation 640 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:954461487" variation 643 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1336455678" variation 645 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658637950" variation 646 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:1377527440" variation 647 /gene="LINC01160" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1658637860" variation 648 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1225840662" variation 650 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658637764" variation 651 /gene="LINC01160" /replace="a" /replace="t" /db_xref="dbSNP:1658637712" variation 652 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:554651926" variation 654 /gene="LINC01160" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1307910830" variation 655 /gene="LINC01160" /replace="a" /replace="t" /db_xref="dbSNP:995249156" variation 666 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1571490690" variation 667 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1571490688" variation 668 /gene="LINC01160" /replace="" /replace="g" /db_xref="dbSNP:1658637431" variation 668 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1316579328" variation 672 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:537838082" variation 677 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658637299" variation 680 /gene="LINC01160" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1030423122" variation 681 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:995822455" variation 686..690 /gene="LINC01160" /replace="ccccc" /replace="cccccc" /db_xref="dbSNP:900419002" variation 686 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1324158565" variation 689 /gene="LINC01160" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:899204000" variation 693..699 /gene="LINC01160" /replace="cc" /replace="ccgcccc" /db_xref="dbSNP:1658636841" variation 694 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:745804415" variation 695 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1007838830" variation 699 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1249318605" variation 700 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:778872576" variation 701 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1557861727" variation 706 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1658636638" variation 709 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1177924373" variation 711 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658636554" variation 712 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:1571490652" variation 713 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1457854521" variation 716..731 /gene="LINC01160" /replace="c" /replace="cccaccagaccccacc" /db_xref="dbSNP:1658636192" variation 720 /gene="LINC01160" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1658636427" variation 722 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658636382" variation 724 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658636331" variation 727 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1470588238" variation 728 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1051948002" variation 734 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658636140" variation 735 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:568955406" variation 736..739 /gene="LINC01160" /replace="ac" /replace="acac" /db_xref="dbSNP:1658635713" variation 737 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:945495240" variation 739 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658635665" variation 746 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1571490647" variation 748 /gene="LINC01160" /replace="a" /replace="t" /db_xref="dbSNP:1658635572" variation 749 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658635523" variation 752 /gene="LINC01160" /replace="t" /replace="tct" /db_xref="dbSNP:1658635466" variation 753 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:1658635424" variation 756..757 /gene="LINC01160" /replace="" /replace="g" /db_xref="dbSNP:1658635301" variation 756 /gene="LINC01160" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1042179635" variation 758..759 /gene="LINC01160" /replace="" /replace="gaacgc" /db_xref="dbSNP:1658635045" variation 758 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:12047884" variation 759 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658635001" variation 760 /gene="LINC01160" /replace="g" /replace="gg" /db_xref="dbSNP:1658634950" variation 764..767 /gene="LINC01160" /replace="" /replace="cttg" /db_xref="dbSNP:1658634841" variation 765 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:1350070197" variation 767..773 /gene="LINC01160" /replace="ggggggg" /replace="gggggggg" /db_xref="dbSNP:1658634314" variation 767 /gene="LINC01160" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1052914661" variation 768 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:539379096" variation 769 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:927280495" variation 771..772 /gene="LINC01160" /replace="" /replace="aggcta" /db_xref="dbSNP:1658634390" variation 773 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1246738901" variation 775 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1658634162" variation 776 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:1658634078" variation 777..778 /gene="LINC01160" /replace="" /replace="g" /db_xref="dbSNP:1658633999" variation 779..784 /gene="LINC01160" /replace="ca" /replace="catcca" /db_xref="dbSNP:1658633831" variation 779 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1380431060" variation 784 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658633755" variation 785 /gene="LINC01160" /replace="a" /replace="t" /db_xref="dbSNP:1658633682" variation 787..793 /gene="LINC01160" /replace="c" /replace="ccatgtc" /db_xref="dbSNP:1658633315" variation 787 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:1658633616" variation 788 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658633550" variation 789 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658633473" variation 790 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:973677694" variation 793 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:925668718" variation 794 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:1658633162" variation 796 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658633085" variation 798 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:1481854770" variation 800..805 /gene="LINC01160" /replace="c" /replace="caaccc" /db_xref="dbSNP:1658632724" variation 800 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1658632932" variation 803 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:963602524" variation 804 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:980154331" variation 806 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658632642" variation 807 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:908057949" variation 815 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658632499" variation 817 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658632427" variation 820 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658632361" variation 822 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:948655241" variation 823 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:1479792484" variation 824 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658632175" variation 825 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658632104" variation 826 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1451973459" variation 827 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:983588895" variation 829 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658631874" variation 830 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658631793" variation 831..832 /gene="LINC01160" /replace="" /replace="tc" /db_xref="dbSNP:1658631729" variation 832..835 /gene="LINC01160" /replace="ct" /replace="ctct" /db_xref="dbSNP:1571490591" variation 832 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:954621217" variation 835..836 /gene="LINC01160" /replace="" /replace="tt" /db_xref="dbSNP:1658631523" variation 838 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:917133765" variation 840 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:1658631391" variation 847 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1030040893" polyA_site 848 /gene="LINC01160" /note="major polyA site" variation 849 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:1331122018" variation 850 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:1658631126" variation 853 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658631060" variation 854 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658630984" variation 864 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658630916" variation 874..875 /gene="LINC01160" /replace="t" /replace="tt" /db_xref="dbSNP:1658630453" variation 875 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1408353572" variation 881 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1658630336" variation 887 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:996326113" variation 893 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:964442823" variation 894 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1164145601" variation 895 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1428058738" variation 906 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658630044" variation 909 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1571490579" variation 910 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1571490576" variation 912 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:188897474" variation 914 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:184577160" variation 915 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:1383894952" variation 916 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1571490562" variation 917 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1435788133" variation 920 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1273183352" variation 921 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:1571490556" variation 928 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:760586430" variation 932 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658629435" variation 937 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1000756727" variation 941 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:950514677" variation 942 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:902411339" variation 945 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:527506201" variation 949 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:561814350" variation 950 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1020752859" variation 951 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1013383218" variation 952 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:1571490529" variation 958 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1218704631" variation 964 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1026563513" variation 966 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:896308786" variation 967 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:548352709" variation 969 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1187685341" variation 971 /gene="LINC01160" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1571490509" variation 972 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658628631" variation 975 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:531312636" variation 978 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1179054174" variation 984 /gene="LINC01160" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:192898273" variation 985 /gene="LINC01160" /replace="a" /replace="t" /db_xref="dbSNP:2101071092" variation 986 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1658628421" variation 988 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:189785217" variation 989 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:545826069" variation 990 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1211374328" variation 991 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1037679929" variation 995 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658628124" variation 996 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1658628062" variation 998 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1405025614" variation 999 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:560625139" variation 1002 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:908088613" variation 1007 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1431380806" variation 1011 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1319743376" variation 1017 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1362974570" variation 1027 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1247852214" variation 1034 /gene="LINC01160" /replace="a" /replace="t" /db_xref="dbSNP:79889603" variation 1035 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:79708365" variation 1038..1042 /gene="LINC01160" /replace="at" /replace="atcat" /db_xref="dbSNP:1658627556" variation 1042 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:1315523192" variation 1050 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:540779956" variation 1051 /gene="LINC01160" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1571490461" variation 1052 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1355184208" variation 1053 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1240864982" variation 1054 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:2101071033" variation 1056 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1471473635" variation 1064 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:781455349" variation 1065 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1030550561" variation 1066 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1440136443" variation 1067 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1658627005" variation 1074 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:1658626949" variation 1076 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:141535763" variation 1079 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:1658626824" variation 1081 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1247897390" variation 1086 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1335355685" variation 1087 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658626668" variation 1089 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1557861610" variation 1090 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1185774642" variation 1094 /gene="LINC01160" /replace="a" /replace="t" /db_xref="dbSNP:1386297121" variation 1096 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658626443" variation 1097 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658626383" variation 1099 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1324499980" variation 1101 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:1571490432" variation 1104 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1472582829" variation 1106 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658626157" variation 1108 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1426922198" variation 1109 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:574972301" variation 1111 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1401311879" variation 1112 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:554639616" variation 1113 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:1571490421" variation 1115 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658625852" variation 1120 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658625804" variation 1122 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1658625755" variation 1123 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658625698" variation 1127 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:1158564968" variation 1131 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:892671223" variation 1132 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:2101070958" variation 1133 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:933543175" variation 1134 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1054347591" variation 1140 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658625415" variation 1141 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658625358" variation 1142 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:755189251" variation 1143 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1337135216" variation 1144 /gene="LINC01160" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1339726179" variation 1145 /gene="LINC01160" /replace="a" /replace="t" /db_xref="dbSNP:1445551475" variation 1149 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658625072" variation 1151 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1571490400" variation 1152 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:1658624951" variation 1154 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1280866067" variation 1155 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658624843" variation 1158 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1350970305" variation 1159 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658624737" variation 1161 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:904246294" variation 1162 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658624604" variation 1163..1167 /gene="LINC01160" /replace="aaaaa" /replace="aaaaaa" /db_xref="dbSNP:1658624512" variation 1163 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:2101070917" variation 1166 /gene="LINC01160" /replace="a" /replace="t" /db_xref="dbSNP:1265739469" variation 1167 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658624453" variation 1169 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658624399" variation 1171..1176 /gene="LINC01160" /replace="aaaaaa" /replace="aaaaaaa" /db_xref="dbSNP:1658624276" variation 1172 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:923426194" variation 1180 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:751715031" variation 1182 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:2101070905" variation 1183 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:974547895" variation 1185 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:2101070903" variation 1188 /gene="LINC01160" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:527691414" variation 1189 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:373684203" variation 1191 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658623932" variation 1192 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:948356332" variation 1193 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1571490380" variation 1197 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1234781780" variation 1198 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1470660415" variation 1199 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1158496551" variation 1203 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:1658623631" variation 1205 /gene="LINC01160" /replace="a" /replace="t" /db_xref="dbSNP:2101070880" variation 1208 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658623581" variation 1211 /gene="LINC01160" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:917166427" variation 1216 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1410820521" variation 1217 /gene="LINC01160" /replace="a" /replace="t" /db_xref="dbSNP:992742953" variation 1218 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1156255225" variation 1219..1230 /gene="LINC01160" /replace="ag" /replace="aggaggctgaag" /db_xref="dbSNP:2101070861" variation 1219 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658623141" variation 1220 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1469212502" variation 1222 /gene="LINC01160" /replace="a" /replace="t" /db_xref="dbSNP:1658623033" variation 1223 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658622980" variation 1229 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:201438539" variation 1234 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1201202149" variation 1240 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1658622786" variation 1241 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1571490360" variation 1243 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:1658622687" variation 1246 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1330672877" variation 1250 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:575214982" variation 1251 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:973620628" variation 1254 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:2101070843" variation 1255 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658622357" variation 1258 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:2101070838" variation 1262 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:979033338" variation 1265 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:184378670" variation 1266 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:963508350" variation 1270 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1223594571" variation 1274 /gene="LINC01160" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:910593284" variation 1275 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:780411689" variation 1278 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658621746" variation 1280 /gene="LINC01160" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1217076619" variation 1282 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1658621561" variation 1288 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:1199066740" variation 1295 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658621388" variation 1299 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:192460333" variation 1301..1303 /gene="LINC01160" /replace="gg" /replace="ggg" /db_xref="dbSNP:1658621180" variation 1303 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1483497380" variation 1308..1311 /gene="LINC01160" /replace="ag" /replace="agag" /db_xref="dbSNP:1020869056" variation 1313 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658620950" variation 1316 /gene="LINC01160" /replace="a" /replace="t" /db_xref="dbSNP:1658620878" variation 1318 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658620830" variation 1321 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1571490324" variation 1326..1332 /gene="LINC01160" /replace="aaaaaaa" /replace="aaaaaaaa" /db_xref="dbSNP:567771881" variation 1329 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1181815759" variation 1330..1335 /gene="LINC01160" /replace="aa" /replace="aaacaa" /db_xref="dbSNP:1350108458" variation 1330 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:568497920" variation 1331..1341 /gene="LINC01160" /replace="aacaacaa" /replace="aacaacaacaa" /db_xref="dbSNP:374240146" variation 1331 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658620601" variation 1333 /gene="LINC01160" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1658620487" variation 1339 /gene="LINC01160" /replace="" /replace="c" /db_xref="dbSNP:1658620387" variation 1339 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:896351590" variation 1340..1346 /gene="LINC01160" /replace="aaaaaa" /replace="aaaaaaa" /db_xref="dbSNP:1397015349" variation 1344 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1169408464" variation 1345 /gene="LINC01160" /replace="a" /replace="t" /db_xref="dbSNP:758741746" variation 1348 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1571490302" variation 1350..1356 /gene="LINC01160" /replace="aaa" /replace="aaataaa" /db_xref="dbSNP:1305722924" variation 1351 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1428696214" variation 1352 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658619997" variation 1353..1358 /gene="LINC01160" /replace="" /replace="taaaat" /db_xref="dbSNP:1658619849" regulatory 1356..1361 /regulatory_class="polyA_signal_sequence" /gene="LINC01160" /note="hexamer: AATAAA" variation 1357 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658619891" regulatory 1360..1365 /regulatory_class="polyA_signal_sequence" /gene="LINC01160" /note="hexamer: AATAAA" variation 1361 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:570687684" variation 1362 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658619740" variation 1363..1367 /gene="LINC01160" /replace="a" /replace="aaaaa" /db_xref="dbSNP:2101070751" variation 1366..1371 /gene="LINC01160" /replace="aat" /replace="aataat" /db_xref="dbSNP:1658619661" variation 1367..1394 /gene="LINC01160" /replace="" /replace="ataatgaatcatgcctatgtaatgaagc" /db_xref="dbSNP:1658618884" variation 1371 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:954733765" variation 1372 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1658619538" polyA_site 1374 /gene="LINC01160" /note="major polyA site" variation 1378 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:1658619453" variation 1380 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:1404989389" variation 1381 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1658619299" polyA_site 1383 /gene="LINC01160" variation 1384 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:905916938" variation 1385 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:1343879049" variation 1387 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:1658619042" variation 1389 /gene="LINC01160" /replace="a" /replace="t" /db_xref="dbSNP:1658618954" variation 1397..1406 /gene="LINC01160" /replace="c" /replace="ccataaaaac" /db_xref="dbSNP:1658618736" variation 1399 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:1658618796" variation 1405..1409 /gene="LINC01160" /replace="aca" /replace="acaca" /db_xref="dbSNP:1658618324" variation 1406 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:7548973" variation 1408 /gene="LINC01160" /replace="" /replace="c" /db_xref="dbSNP:1658618383" variation 1409..1415 /gene="LINC01160" /replace="aa" /replace="aaaagaa" /db_xref="dbSNP:1658618159" variation 1409..1412 /gene="LINC01160" /replace="aa" /replace="aaaa" /db_xref="dbSNP:1658618281" variation 1409 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:1401017282" variation 1413 /gene="LINC01160" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:138571930" variation 1415 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1048008997" variation 1421 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:568290360" variation 1425..1427 /gene="LINC01160" /replace="gg" /replace="ggg" /db_xref="dbSNP:1658617987" variation 1425 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1272691170" variation 1430 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1658617930" variation 1436 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:957157298" variation 1439 /gene="LINC01160" /replace="a" /replace="t" /db_xref="dbSNP:1032526860" variation 1440 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658617758" variation 1451 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:933555465" variation 1454 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1425336399" variation 1455 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1001410959" variation 1456 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:904278207" variation 1464 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:186710461" variation 1466 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658617440" variation 1469 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:1266823930" variation 1471 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1557861515" variation 1473 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:923482430" variation 1478 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:761278227" variation 1480 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1195320133" variation 1482 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658617140" variation 1484 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1390713791" variation 1493 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658617023" variation 1497 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658616974" variation 1500 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1479217042" variation 1501 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:1166519331" variation 1502..1506 /gene="LINC01160" /replace="tttt" /replace="ttttt" /db_xref="dbSNP:1658616818" variation 1502 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:2101070665" variation 1509 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658616762" variation 1510 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1571490230" variation 1512 /gene="LINC01160" /replace="g" /replace="t" /db_xref="dbSNP:1658616663" variation 1513 /gene="LINC01160" /replace="a" /replace="c" /db_xref="dbSNP:1658616605" variation 1515 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1428189061" variation 1516 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1386677332" variation 1518..1521 /gene="LINC01160" /replace="c" /replace="cctc" /db_xref="dbSNP:1658616331" variation 1518 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1424957697" variation 1519 /gene="LINC01160" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1292426198" variation 1522 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658616278" variation 1525 /gene="LINC01160" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1658616233" variation 1526 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:531400593" variation 1527 /gene="LINC01160" /replace="c" /replace="t" /db_xref="dbSNP:1658616124" variation 1529 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1194063366" variation 1533 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1044085043" variation 1534 /gene="LINC01160" /replace="c" /replace="g" /db_xref="dbSNP:1658615984" variation 1539 /gene="LINC01160" /replace="a" /replace="t" /db_xref="dbSNP:1012616546" variation 1541 /gene="LINC01160" /replace="a" /replace="g" /db_xref="dbSNP:1658615890" variation 1542 /gene="LINC01160" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1658615841" ORIGIN
tctctgcccggccgcccatcgtctgagatgtggggagagcctctgccccgccgccccgcctgggatgtgaggagcgcctctacccggccgcgaccccgtctgggaggtgaggagcgtctctgcccggccgccccgtctgagaagtgaggagaccctccgcctcgcagccgccccgtctgaaaaggtggctgtcaatagattggcccaaaaggaagaacaaggaaaagggcaccaaagaagataaatgaaaatacaagggtataagctgaactgtggacatcctgccactgggaattaagttaaagtagaaaaaagcagaatgtaatggggagtcccctcacaagaagaatttggatcaaagcatggcagtgaggggaagcattgagcagtgccgatttcaaatgaagactgacttgatcctgaacataacctacaagaagaaagggaccacaggctatacacaaagcatggtgccggcatctgcttctggtgagggcctcaggaagcttacaatcatcttggaaggtgaagaggaagccagcgcatcacatggcaagagagggagcaagagagaaggggacagtgccgcacactttaaaaaaaaaccttatctcacgaggcagaactaactgagtgagagttcactcatcaccaagggaatggtgctgagtcattcatgagggatccccctgccgcccccgtgatccaatcacctcccaccagaccccacctccaacactggggattacatttcaacatgagacttgggggggacaaacatccaaaccatgtcagtcttcaacccctcttcctgacatacaactcctaaaactcttagaatctccaaagtgctgtctttttatgtgttagtaattggctagtggctcacagccccttggtagcttcaggatggggcctggtcactggaaagaccaagtcataattagagggttgagactttcagcccacccccaacatctggggagaagagaagggccgaagctcaaattgatcaccaatggccagtgttttaattaatcatgtggccaggcgtggtggctcacgcctgtaatcctagcactttgggaggctgaggcaggtggatcacgaggtcaggagatggagaccatcctggctaacacggtgaaactccatctctactaaaaatacaaaaaattagctggatgcggtggcatgcgcctgtagtcccagctactcaggaggctgaagcaggagaatcacttgaacccgggaggcagaggttacagtgagccgagattacaccactgcactccagcctgggtgacagagccagactccatctcaaaaaaacaacaacaaaaaaagacaaataaaataaataaaaataatgaatcatgcctatgtaatgaagcctccataaaaacacaaaagaatagggttcagggagcctctggatagctgaatatctggaggctcctagagagtggcatgtccagagggcatggaagctctgtgcccctttttcaccctatacacctcatcatctgtatgcttggtaat
//
by
@meso_cacase at
DBCLS
This page is licensed under a
Creative Commons Attribution 4.0 International License (CC BY 4.0).
If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596.
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